Research output per year
Research output per year
- 1 - 50 out of 134 results
Search results
-
2024
The Clinical Development of Taldefgrobep Alfa: An Anti-Myostatin Adnectin for the Treatment of Duchenne Muscular Dystrophy
the Taldefgrobep Alfa Study Group, Feb 2024, In: Neurology and Therapy. 13, 1, p. 183-219 37 p.Research output: Contribution to journal › Article › peer-review
Open Access -
2023
Correction to: Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study (Neurology and Therapy, (2023), 12, 2, (543-557), 10.1007/s40120-023-00444-1)
the JEWELFISH Study Group, Oct 2023, In: Neurology and Therapy. 12, 5, p. 1799-1801 3 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
Lean tissue mass measurements by dual-energy X-ray absorptiometry and associations with strength and functional outcome measures in facioscapulohumeral muscular dystrophy
the ReSolve Investigators of the FSHD CTRN, Sep 2023, In: Neuromuscular Disorders. 33, 9, p. 63-68 6 p.Research output: Contribution to journal › Article › peer-review
-
Microdystrophin Expression as a Surrogate Endpoint for Duchenne Muscular Dystrophy Clinical Trials
Chamberlain, J. S., Robb, M., Braun, S., Brown, K. J., Danos, O., Ganot, A., Gonzalez-Alegre, P., Hunter, N., McDonald, C., Morris, C., Tobolowsky, M., Wagner, K. R., Ziolkowski, O. & Duan, D., May 1 2023, In: Human gene therapy. 34, 9-10, p. 404-415 12 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study
the JEWELFISH Study Group, Apr 2023, In: Neurology and Therapy. 12, 2, p. 543-557 15 p.Research output: Contribution to journal › Article › peer-review
Open Access -
2022
A Combined Prospective and Retrospective Comparison of Long-Term Functional Outcomes Suggests Delayed Loss of Ambulation and Pulmonary Decline with Long-Term Eteplirsen Treatment
Mitelman, O., Abdel-Hamid, H. Z., Byrne, B. J., Connolly, A. M., Heydemann, P., Proud, C., Shieh, P. B., Wagner, K. R., Dugar, A., Santra, S., Signorovitch, J., Goemans, N., McDonald, C. M., Mercuri, E. & Mendell, J. R., 2022, In: Journal of neuromuscular diseases. 9, 1, p. 39-52 14 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy
Sherlock, S. P., Palmer, J., Wagner, K. R., Abdel-Hamid, H. Z., Tian, C., Mah, J. K., Muntoni, F., Guglieri, M., Butterfield, R. J., Charnas, L. & Marraffino, S., Dec 2022, In: Scientific reports. 12, 1, 18762.Research output: Contribution to journal › Article › peer-review
Open Access -
Engineering Skeletal Muscle Grafts with PAX7::GFP-Sorted Human Pluripotent Stem Cell-Derived Myogenic Progenitors on Fibrin Microfiber Bundles for Tissue Regeneration
Somers, S. M., Gilbert-Honick, J., Choi, I. Y., K. W. Lo, E., Lim, H. T., Dias, S., Wagner, K. R., Mao, H. Q., Cahan, P., Lee, G. & Grayson, W. L., Nov 2022, In: Bioengineering. 9, 11, 693.Research output: Contribution to journal › Article › peer-review
Open Access -
Home-based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy
Gidaro, T., Gasnier, E., Annoussamy, M., Vissing, J., Attarian, S., Mozaffar, T., Iyadurai, S., Wagner, K. R., Vissière, D., Walker, G., Shukla, S. S. & Servais, L., Feb 2022, In: Muscle and Nerve. 65, 2, p. 237-242 6 p.Research output: Contribution to journal › Article › peer-review
-
Human pluripotent stem cell-derived myogenic progenitors undergo maturation to quiescent satellite cells upon engraftment
Sun, C., Kannan, S., Choi, I. Y., Lim, H. T., Zhang, H., Chen, G. S., Zhang, N., Park, S. H., Serra, C., Iyer, S. R., Lloyd, T. E., Kwon, C., Lovering, R. M., Lim, S. B., Andersen, P., Wagner, K. R. & Lee, G., Apr 7 2022, In: Cell stem cell. 29, 4, p. 610-619.e5Research output: Contribution to journal › Article › peer-review
Open Access -
iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modeling
Guo, D., Daman, K., Chen, J. J., Shi, M. J., Yan, J., Matijasevic, Z., Rickard, A. M., Bennett, M. H., Kiselyov, A., Zhou, H., Bang, A. G., Wagner, K. R., Maehr, R., King, O. D., Hayward, L. J. & Emerson, C. P., Jan 2022, In: eLife. 11, e70341.Research output: Contribution to journal › Article › peer-review
Open Access -
Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis
Britson, K. A., Ling, J. P., Braunstein, K. E., Montagne, J. M., Kastenschmidt, J. M., Wilson, A., Ikenaga, C., Tsao, W., Pinal-Fernande, I., Russell, K. A., Reed, N., Mozaffar, T., Wagner, K. R., Ostrow, L. W., Corse, A. M., Mammen, A. L., Villalta, S. A., Larman, H. B., Wong, P. C. & Lloyd, T. E., Jan 19 2022, In: Science translational medicine. 14, 628, eabi9196.Research output: Contribution to journal › Article › peer-review
Open Access -
Novel approaches to analysis of the North Star Ambulatory Assessment (NSAA) in Duchenne muscular dystrophy (DMD): Observations from a phase 2 trial
Muntoni, F., Guglieri, M., Mah, J. K., Wagner, K. R., Brandsema, J. F., Butterfield, R. J., McDonald, C. M., Mayhew, A. G., Palmer, J. P., Marraffino, S., Charnas, L. & Mercuri, E., Aug 2022, In: PloS one. 17, 8 August, e0272858.Research output: Contribution to journal › Article › peer-review
Open Access -
Piezo1: opening the way to preventing muscle atrophy
Jagasia, R. & Wagner, K. R., May 16 2022, In: Journal of Clinical Investigation. 132, 10, e159668.Research output: Contribution to journal › Article › peer-review
Open Access -
Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab
Sherlock, S. P., Palmer, J., Wagner, K. R., Abdel-Hamid, H. Z., Bertini, E., Tian, C., Mah, J. K., Kostera-Pruszczyk, A., Muntoni, F., Guglieri, M., Brandsema, J. F., Mercuri, E., Butterfield, R. J., McDonald, C. M., Charnas, L. & Marraffino, S., Aug 2022, In: Journal of neurology. 269, 8, p. 4421-4435 15 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Quantitative muscle analysis in facioscapulohumeral muscular dystrophy using whole-body fat-referenced MRI: Protocol development, multicenter feasibility, and repeatability
Widholm, P., Ahlgren, A., Karlsson, M., Romu, T., Tawil, R., Wagner, K. R., Statland, J. M., Wang, L. H., Shieh, P. B., van Engelen, B. G. M., Cadavid, D., Ronco, L., Odueyungbo, A. O., Jiang, J. G., Mellion, M. L. & Dahlqvist Leinhard, O., Aug 2022, In: Muscle and Nerve. 66, 2, p. 183-192 10 p.Research output: Contribution to journal › Article › peer-review
-
Quantitative Muscle Analysis in FSHD Using Whole-Body Fat-Referenced MRI: Composite Scores for Longitudinal and Cross-sectional Analysis
Mellion, M. L., Widholm, P., Karlsson, M., Ahlgren, A., Tawil, R., Wagner, K. R., Statland, J. M., Wang, L., Shieh, P. B., Van Engelen, B. G. M., Kools, J., Ronco, L., Odueyungbo, A., Jiang, J., Han, J. J., Hatch, M., Towles, J., Leinhard, O. D. & Cadavid, D., Aug 30 2022, In: Neurology. 99, 9, p. E877-E889Research output: Contribution to journal › Article › peer-review
-
Randomized phase 2 study of ACE-083, a muscle-promoting agent, in facioscapulohumeral muscular dystrophy
Statland, J. M., Campbell, C., Desai, U., Karam, C., Díaz-Manera, J., Guptill, J. T., Korngut, L., Genge, A., Tawil, R. N., Elman, L., Joyce, N. C., Wagner, K. R., Manousakis, G., Amato, A. A., Butterfield, R. J., Shieh, P. B., Wicklund, M., Gamez, J., Bodkin, C., Pestronk, A., & 9 others, Jul 2022, In: Muscle and Nerve. 66, 1, p. 50-62 13 p.Research output: Contribution to journal › Article › peer-review
Open Access -
2021
A phase Ib/IIa, open-label, multiple ascending-dose trial of domagrozumab in fukutin-related protein limb-girdle muscular dystrophy
Leung, D. G., Bocchieri, A. E., Ahlawat, S., Jacobs, M. A., Parekh, V. S., Braverman, V., Summerton, K., Mansour, J., Stinson, N., Bibat, G., Morris, C., Marraffino, S. & Wagner, K. R., Aug 2021, In: Muscle and Nerve. 64, 2, p. 172-179 8 p.Research output: Contribution to journal › Article › peer-review
-
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial
Finkel, R. S., McDonald, C. M., Lee Sweeney, H., Finanger, E., Neil Knierbein, E., Wagner, K. R., Mathews, K. D., Marks, W., Statland, J., Nance, J., McMillan, H. J., McCullagh, G., Tian, C., Ryan, M. M., O'Rourke, D., Müller-Felber, W., Tulinius, M., Burnette, W. B., Nguyen, C. T., Vijayakumar, K., & 6 others, 2021, In: Journal of neuromuscular diseases. 8, 5, p. 769-784 16 p.Research output: Contribution to journal › Article › peer-review
Open Access -
CaMKII oxidation is a critical performance/disease trade-off acquired at the dawn of vertebrate evolution
Wang, Q., Hernández-Ochoa, E. O., Viswanathan, M. C., Blum, I. D., Do, D. C., Granger, J. M., Murphy, K. R., Wei, A. C., Aja, S., Liu, N., Antonescu, C. M., Florea, L. D., Talbot, C. C., Mohr, D., Wagner, K. R., Regot, S., Lovering, R. M., Gao, P., Bianchet, M. A., Wu, M. N., & 4 others, Dec 1 2021, In: Nature communications. 12, 1, 3175.Research output: Contribution to journal › Article › peer-review
Open Access -
Corrigendum to “Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy” [Neuromuscular Disorders, Vol. 30 (6) 2020, 492-502] (Neuromuscular Disorders (2020) 30(6) (492–502), (S0960896620301188), (10.1016/j.nmd.2020.05.002))
Wagner, K. R., Abdel-Hamid, H. Z., Mah, J. K., Campbell, C., Guglieri, M., Muntoni, F., Takeshima, Y., McDonald, C. M., Kostera-Pruszczyk, A., Karachunski, P., Butterfield, R. J., Mercuri, E., Fiorillo, C., Bertini, E. S., Tian, C., Statland, J., Sadosky, A. B., Purohit, V. S., Sherlock, S. P., Palmer, J. P., & 4 others, Feb 2021, In: Neuromuscular Disorders. 31, 2, p. 167-168 2 p.Research output: Contribution to journal › Comment/debate › peer-review
1 Scopus citations -
Human muscle stem cells are refractory to aging
Novak, J. S., Mázala, D. A. G., Nearing, M., Hindupur, R., Uapinyoying, P., Habib, N. F., Dickson, T., Ioffe, O. B., Harris, B. T., Fidelia-Lambert, M. N., Rossi, C. T., Hill, D. A., Wagner, K. R., Hoffman, E. P. & Partridge, T. A., Jul 2021, In: Aging Cell. 20, 7, e13411.Research output: Contribution to journal › Article › peer-review
Open Access -
Mss51 deletion increases endurance and ameliorates histopathology in the mdx mouse model of Duchenne muscular dystrophy
Rovira Gonzalez, Y. I., Moyer, A. L., LeTexier, N. J., Bratti, A. D., Feng, S., Peña, V., Sun, C., Pulcastro, H., Liu, T., Iyer, S. R., Lovering, R. M., O'Rourke, B. & Wagner, K. R., Feb 2021, In: FASEB Journal. 35, 2, e21276.Research output: Contribution to journal › Article › peer-review
-
Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping: PROMOVI Trial
McDonald, C. M., Shieh, P. B., Abdel-Hamid, H. Z., Connolly, A. M., Ciafaloni, E., Wagner, K. R., Goemans, N., Mercuri, E., Khan, N., Koenig, E., Malhotra, J., Zhang, W., Han, B. & Mendell, J. R., 2021, In: Journal of neuromuscular diseases. 8, 6, p. 989-1001 13 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Progress in repairing muscle
Wagner, K. R., Nov 2021, In: Seminars in Cell and Developmental Biology. 119, p. 1-2 2 p.Research output: Contribution to journal › Editorial › peer-review
-
Safety, tolerability, and pharmacokinetics of casimersen in patients with Duchenne muscular dystrophy amenable to exon 45 skipping: A randomized, double-blind, placebo-controlled, dose-titration trial
Wagner, K. R., Kuntz, N. L., Koenig, E., East, L., Upadhyay, S., Han, B. & Shieh, P. B., Sep 2021, In: Muscle and Nerve. 64, 3, p. 285-292 8 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Safety and disease monitoring biomarkers in Duchenne muscular dystrophy: Results from a Phase II trial
Wagner, K. R., Guglieri, M., Ramaiah, S. K., Charnas, L., Marraffino, S., Binks, M., Vaidya, V. S., Palmer, J., Goldstein, R. & Muntoni, F., Oct 2021, In: Biomarkers in Medicine. 15, 15, p. 1389-1396 8 p.Research output: Contribution to journal › Article › peer-review
Open Access -
2020
A decade of optimizing drug development for rare neuromuscular disorders through TACT
Wagner, K. R., De Luca, A., Caizergues, D., Dowling, J., Goemans, N., Gordish-Dressman, H., Grounds, M. D., Kelly, M., Mayhew, A., McNally, E. M., Zoetis, T., Lee, J., Turner, C., Wells, D. J., Csimma, C. & Straub, V., Jan 1 2020, In: Nature Reviews Drug Discovery. 19, 1Research output: Contribution to journal › Comment/debate › peer-review
Open Access2 Scopus citations -
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Lek, A., Zhang, Y., Woodman, K. G., Huang, S., DeSimone, A. M., Cohen, J., Ho, V., Conner, J., Mead, L., Kodani, A., Pakula, A., Sanjana, N., King, O. D., Jones, P. L., Wagner, K. R., Lek, M. & Kunkel, L. M., Mar 25 2020, In: Science translational medicine. 12, 536, eaay0271.Research output: Contribution to journal › Article › peer-review
8 Scopus citations -
Diabetes, metformin and cancer risk in myotonic dystrophy type I
Alsaggaf, R., Pfeiffer, R. M., Wang, Y., St. George, D. M. M., Zhan, M., Wagner, K. R., Amr, S., Greene, M. H. & Gadalla, S. M., Aug 1 2020, In: International Journal of Cancer. 147, 3, p. 785-792 8 p.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Duchenne muscular dystrophy hiPSC–derived myoblast drug screen identifies compounds that ameliorate disease in mdx mice
Sun, C., Choi, I. Y., Rovira Gonzalez, Y. I., Andersen, P., Conover Talbot, C., Iyer, S. R., Lovering, R. M., Wagner, K. R. & Lee, G., Jun 4 2020, In: JCI Insight. 5, 11, e134287.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Engineering 3D skeletal muscle primed for neuromuscular regeneration following volumetric muscle loss
Gilbert-Honick, J., Iyer, S. R., Somers, S. M., Takasuka, H., Lovering, R. M., Wagner, K. R., Mao, H. Q. & Grayson, W. L., Oct 2020, In: Biomaterials. 255, 120154.Research output: Contribution to journal › Article › peer-review
7 Scopus citations -
Improving translatability of preclinical studies for neuromuscular disorders: Lessons from the TREAT-NMD Advisory Committee for Therapeutics (TACT)
Willmann, R., Lee, J., Turner, C., Nagaraju, K., Aartsma-Rus, A., Wells, D. J., Wagner, K. R., Csimma, C., Straub, V., Grounds, M. D. & de Luca, A., 2020, In: DMM Disease Models and Mechanisms. 13, 2, dmm042903.Research output: Contribution to journal › Review article › peer-review
Open Access7 Scopus citations -
It's not all about muscle: Fibroadipogenic progenitors contribute to facioscapulohumeral muscular dystrophy
Serra, C. & Wagner, K. R., May 1 2020, In: Journal of Clinical Investigation. 130, 5, p. 2186-2188 3 p.Research output: Contribution to journal › Review article › peer-review
Open Access2 Scopus citations -
Longitudinal functional and imaging outcome measures in FKRP limb-girdle muscular dystrophy
Leung, D. G., Bocchieri, A. E., Ahlawat, S., Jacobs, M. A., Parekh, V. S., Braverman, V., Summerton, K., Mansour, J., Bibat, G., Morris, C., Marraffino, S. & Wagner, K. R., May 19 2020, In: BMC neurology. 20, 1, 196.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Meeting report: the 2020 FSHD International Research Congress
Kyba, M., Bloch, R. J., Dumonceaux, J., Harper, S. Q., van der Maarel, S. M., Sverdrup, F. M., Wagner, K. R., van Engelen, B. & Chen, Y. W., Dec 2020, In: Skeletal Muscle. 10, 1, 36.Research output: Contribution to journal › Article › peer-review
Open Access -
Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy
Wagner, K. R., Abdel-Hamid, H. Z., Mah, J. K., Campbell, C., Guglieri, M., Muntoni, F., Takeshima, Y., McDonald, C. M., Kostera-Pruszczyk, A., Karachunski, P., Butterfield, R. J., Mercuri, E., Fiorillo, C., Bertini, E. S., Tian, C., Statland, J., Sadosky, A. B., Purohit, V. S., Sherlock, S. P., Palmer, J. P., & 4 others, Jun 2020, In: Neuromuscular Disorders. 30, 6, p. 492-502 11 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Stem cell-based therapies for Duchenne muscular dystrophy
Sun, C., Serra, C., Lee, G. & Wagner, K. R., Jan 2020, In: Experimental Neurology. 323, 113086.Research output: Contribution to journal › Review article › peer-review
Open Access25 Scopus citations -
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic
Veerapandiyan, A., Wagner, K. R., Apkon, S., McDonald, C. M., Mathews, K. D., Parsons, J. A., Wong, B. L., Eichinger, K., Shieh, P. B., Butterfield, R. J., Rao, V. K., Smith, E. C., Proud, C. M., Connolly, A. M. & Ciafaloni, E., Jul 1 2020, In: Muscle and Nerve. 62, 1, p. 41-45 5 p.Research output: Contribution to journal › Article › peer-review
Open Access21 Scopus citations -
The elusive promise of myostatin inhibition for muscular dystrophy
Wagner, K. R., Oct 1 2020, In: Current opinion in neurology. 33, 5, p. 621-628 8 p.Research output: Contribution to journal › Review article › peer-review
Open Access5 Scopus citations -
2019
AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice
Nance, M. E., Shi, R., Hakim, C. H., Wasala, N. B., Yue, Y., Pan, X., Zhang, T., Robinson, C. A., Duan, S. X., Yao, G., Yang, N. N., Chen, S. J., Wagner, K. R., Gersbach, C. A. & Duan, D., Sep 4 2019, In: Molecular Therapy. 27, 9, p. 1568-1585 18 p.Research output: Contribution to journal › Article › peer-review
Open Access17 Scopus citations -
Benign tumors in myotonic dystrophy type I target disease-related cancer sites
Alsaggaf, R., St. George, D. M. M., Zhan, M., Pfeiffer, R. M., Wang, Y., Anderson, L. A., Liu, Z., Koshiol, J., Bauer, A. J., Wagner, K. R., Greene, M. H., Amr, S. & Gadalla, S. M., 2019, In: Annals of Clinical and Translational Neurology. 6, 8, p. 1510-1518 9 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Clinical trial readiness to solve barriers to drug development in FSHD (ReSolve): Protocol of a large, international, multi-center prospective study
Lorusso, S., Johnson, N. E., McDermott, M. P., Eichinger, K., Butterfield, R. J., Carraro, E., Higgs, K., Lewis, L., Mul, K., Sacconi, S., Sansone, V. A., Shieh, P., Van Engelen, B., Wagner, K., Wang, L., Statland, J. M., Tawil, R., Dimachkie, M., Pasnoor, M., Roath, K., & 32 others, Sep 10 2019, In: BMC neurology. 19, 1, 224.Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
Design of Clinical Trials for Gene Therapy in Muscular Dystrophy
Quiroz, J. & Wagner, K., Jan 1 2019, Muscle Gene Therapy, Second Edition. Springer International Publishing, p. 667-680 14 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
-
Engineering 3D skeletal muscle primed for neuromuscular regeneration following volumetric muscle loss
Gilbert-Honick, J., Wagner, K. R., Mao, H. Q. & Grayson, W. L., Jan 1 2019, Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence - Transactions of the 42nd Annual Meeting. Society for Biomaterials, 1 p. (Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium; vol. 40).Research output: Chapter in Book/Report/Conference proceeding › Conference contribution
-
Facioscapulohumeral Muscular Dystrophies
Wagner, K. R., Dec 1 2019, In: CONTINUUM Lifelong Learning in Neurology. 25, 6, p. 1662-1681 20 p.Research output: Contribution to journal › Review article › peer-review
6 Scopus citations -
Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
DeSimone, A. M., Leszyk, J., Wagner, K. & Emerson, C. P., Dec 11 2019, In: Science Advances. 5, 12, eaaw7099.Research output: Contribution to journal › Article › peer-review
Open Access10 Scopus citations -
Long-read single-molecule maps of the functional methylome
Sharim, H., Grunwald, A., Gabrieli, T., Michaeli, Y., Margalit, S., Torchinsky, D., Arielly, R., Nifker, G., Juhasz, M., Gularek, F., Almalvez, M., Dufault, B., Chandra, S. S., Liu, A., Bhattacharya, S., Chen, Y. W., Vilain, E., Wagner, K. R., Pevsner, J., Reifenberger, J., & 6 others, Apr 2019, In: Genome research. 29, 4, p. 646-656 11 p.Research output: Contribution to journal › Article › peer-review
Open Access12 Scopus citations -
Mss51 deletion enhances muscle metabolism and glucose homeostasis in mice
Rovira Gonzalez, Y. I., Moyer, A. L., LeTexier, N. J., Bratti, A. D., Feng, S., Sun, C., Liu, T., Mula, J., Jha, P., Iyer, S. R., Lovering, R., O’Rourke, B., Noh, H. L., Suk, S., Kim, J. K., Essien Umanah, G. K. & Wagner, K. R., Sep 17 2019, In: JCI Insight. 4, 20, e122247.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations